A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576364



Internal ID16363773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295812..5296552hg38UCSC Ensembl
Innerchr18:5295811..5296551hg19UCSC Ensembl
Innerchr18:5285811..5286551hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38741
hg19741
hg18741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877679, nssv877680
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576364
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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